A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489683



Internal ID21147236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:44893702..44894442hg38UCSC Ensembl
chr14:45362905..45363645hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38741
hg19741
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18018727
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489683
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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